Richards-Rundle syndrome (Q60243): Difference between revisions

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Síndrome de Richards-Rundle é um transtorno muito raro caracterizado por ataxia autossômica recessiva, perda auditiva, deterioração mental, perda muscular periférica, hipogonadismo hipergonadotrófico e cetoacidúria.
description / endescription / en
 
Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria.
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Property / Canonical URI: https://id.who.int/icd/entity/114583632 / rank
 
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Property / CURIE
 
CID11:ID_114583632
Property / CURIE: CID11:ID_114583632 / rank
 
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Property / Canary Token
 
dki-india-ID_114583632
Property / Canary Token: dki-india-ID_114583632 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
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Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 07:45, 14 August 2026

Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria.
Language Label Description Also known as
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ID_114583632
    English
    Richards-Rundle syndrome
    Richards-Rundle syndrome is a very rare disorder characterised by autosomal recessive ataxia, hearing loss, mental deterioration, peripheral muscle wasting, hypergonadotrophic hypogonadism and ketoaciduria.

      Statements

      CID11:ID_114583632
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      dki-india-ID_114583632
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      Concluído
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      13 August 2026
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